80353
TDA Reagent
suitable for microbiology
Synonym(s):
Iron(III) chloride solution, Tryptophan Deaminase Reagent, Ferric chloride solution
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
FeCl3
CAS Number:
Molecular Weight:
162.20
NACRES:
NA.85
PubChem Substance ID:
UNSPSC Code:
41171621
MDL number:
agency
according to ISO 10273:2017
Quality Level
product line
BioChemika
form
liquid
shelf life
limited shelf life, expiry date on the label
composition
ferric chloride, 1 g/10 mL (in distilled water)
technique(s)
microbe id | specific enzyme detection: suitable
application(s)
clinical testing
food and beverages, microbiology
suitability
Proteus spp.
SMILES string
Cl[Fe](Cl)Cl
InChI
1S/3ClH.Fe/h3*1H;/q;;;+3/p-3
InChI key
RBTARNINKXHZNM-UHFFFAOYSA-K
Application
For identification of Proteus species by detection of tryptophan deaminase activity.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2
Storage Class
12 - Non Combustible Liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
Chen-Yu Chen et al.
Clinica chimica acta; international journal of clinical chemistry, 438, 337-341 (2014-10-05)
Insulin-like growth factor binding protein-1 (IGFBP-1) constitutes a subgroup of the insulin-like growth factor binding protein systems, and its concentration in amniotic fluid is 100-1000 times higher than the concentration in other body fluids. The aim of this study was
Abdelwareth A O Sarhan et al.
Chemical Society reviews, 38(9), 2730-2744 (2009-08-20)
In this critical review, the use of iron(III) chloride in oxidative C-C couplings of arenes and related unsaturated compounds is presented and reviewed. The approach allows highly selective dimerisations of phenol derivatives, naphthols, and heterocyclic compounds. Sequential couplings give access
Dattatraya H Dethe et al.
Organic letters, 15(3), 429-431 (2013-01-16)
A novel approach was developed for the synthesis of highly substituted indene derivatives, using an FeCl(3) catalyzed Prins-type cyclization reaction which was further applied in the total synthesis of jungianol and epi-jungianol.